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1.
Article in English | IMSEAR | ID: sea-31518

ABSTRACT

Leptospirosis is an emerging health problem in Thailand, with dramatic increases in reported incidence since 1996. The annual number of reported leptospirosis cases increased from 398 cases in 1996 to 14,285 cases in 2000. In 2001, 2002, and 2003, the number of reported cases decreased, but still remained high at 10,217, 6,864, and 4,958 cases, respectively. The epidemiological characteristics of leptospirosis in Thailand include a peak incidence in September and October in association with the rainy season. A vast majority of the cases (90%) were reported in the Northeast region. The case fatality rate was as high as 4.4%, having a predominant association with male farmers aged 15 to 45 years. Outpatient cases were approximately 9 times more common than admitted cases, with an apparent recent shift in the pattern of infecting serovars among reservoir animals and humans.


Subject(s)
Adolescent , Adult , Agriculture , Animals , Child , Child, Preschool , Communicable Diseases, Emerging/epidemiology , Female , Geography , Humans , Incidence , Leptospirosis/epidemiology , Male , Middle Aged , Rodentia/microbiology , Seasons , Thailand/epidemiology , Zoonoses/epidemiology
2.
Article in English | IMSEAR | ID: sea-32799

ABSTRACT

An easy, rapid and robust dipstick assay for detection of leptospira-specific immunoglobulin M (IgM) antibodies was evaluated on 403 patients admitted for hospitalization because of fever. The clinical symptoms and signs of 35 patients were consistent with leptospirosis. The final diagnosis for the remaining patients was as follows: 136 with typhoid fever, 82 with hepatitis, 74 with malaria, 48 with infections of the respiratory tract, and 20 with fever of unknown origin. The clinical diagnosis of leptospirosis was confirmed for 24 (68.6%) patients by the combined results of the microscopic agglutination test (MAT), the reference test for leptospirosis, and of IgM ELISA, a standard laboratory test for the serodiagnosis of leptospirosis. In addition, serum specimens from 8 (2.2%) patients with a final clinical diagnosis other than leptospirosis were found to be positive in MAT and/or IgM ELISA. Compared with the results of MAT and IgM ELISA a sensitivity of 91.6% and specificity of 93.6% was calculated for the dipstick assay. Most of the serum samples from the laboratory confirmed patients gave a moderate to strong staining intensity of the antigen band of the dipstick and were easy to read. The results demonstrate that the dipstick assay is convenient to use and allows the rapid and accurate confirmation of patients with clinical suspicion of leptospirosis in areas where the disease is endemic.


Subject(s)
Antibodies, Bacterial/urine , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin M/urine , Indonesia , Leptospira/immunology , Leptospirosis/diagnosis , Sensitivity and Specificity , Serologic Tests/methods
3.
West Indian med. j ; West Indian med. j;42(4): 144-6, Dec. 1993.
Article in English | LILACS | ID: lil-130557

ABSTRACT

Paraffinized tissue from Barbadian women with histologically proven gential carcinoma was subjected to a censensus polymerase chain reaction method. Nineteen patients had cervical and one, vaginal carcinoma. The histological types were 17 squamous cell carcinoma, 2 adenocarcinoma and 1 adenosquamous carcinoma. HPVDNA was detected in 18/20 (90 per cent ). HPVDNA type 16 in 13 (65 per cent ), type 33 and type 45 in 1 (5 per cent ) each and 3 (15 per cent ) could not be typed. HPVDNA, type 16, was detected in one (50 per cent ) of the two cases of adenocarcinoma and 12/17 (71 per cent ) cases of squamous cell carcinoma. DNAHPV, type 33, and type 45 were each detected in 1/17 (6 per cent ) cases of squamous cell carcinoma. No HPVDNA, type 18, was detected.


Subject(s)
Humans , Adult , Middle Aged , Female , Papillomaviridae/genetics , Vaginal Neoplasms/microbiology , DNA, Viral , Uterine Cervical Neoplasms/microbiology , Oncogenic Viruses , Barbados , Carcinoma, Squamous Cell/microbiology , DNA Probes, HPV , Adenocarcinoma/microbiology , Polymerase Chain Reaction
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